Abnormalities of Gq-mediated cell signaling in Bartter and Gitelman syndromes1*1See Editorial by Warnock, p. 1197
Author:
Publisher
Elsevier BV
Subject
Nephrology
Reference34 articles.
1. Gitelman's variant of Bartter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl cotransporter;Simon;Nat Genet,1996
2. Bartter's syndrome, hypokalaemic alkalosis with hypercalciuria, is caused by mutations in the Na-K-2Cl cotransporter NKCC2;Simon;Nat Genet,1996
3. Genetic heterogeneity of Bartter's syndrome revealed by mutations in the K+ channel: ROMK;Simon;Nat Genet,1996
4. Mutation in the chloride channel gene CLCNKB causes Bartter's syndrome type III;Simon;Nat Genet,1997
5. The molecular basis of inherited hypokalemic alkalosis: Bartter's and Gitelman's syndromes;Simon;Am J Physiol,1996
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